ISO 9000 Quality Management Systems

Friday, September 12, 2008

SQA is a professional services company that specializes in supplier quality management. Put simply, we help our clients make things better. We operate across a broad industry spectrum, typically in areas that are highly regulated, high precision or high value, examples include:

Medical Devices
Aerospace & Defense
High-Tech
Pharmaceutical
Automotive
Oil & Gas

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Manufacturer's Responsibility

Responsibility of manufacturers

The CE marking must be affixed by the manufacturer or his agent established within the Community. The manufacturer bears ultimate responsibility for the conformity of the product.

Conformity assessment relates to the design and production phases of the product. Depending on the conformity assessment procedures applied, a notified body may be involved in these two phases. If the notified body is involved in the production control phase, its identification number will follow the CE marking.

If a product falls within the scope of a directive that provides for the CE marking, this should be affixed:

to all new products, whether manufactured in the Member States or in third countries;
to used and second hand products imported from third countries.

“There is only one boss. The customer. And he can fire everybody in the company from the chairman on down, simply by spending his money somewhere else.”
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ISO 9000 Quality Management Systems

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Friday, September 12, 2008

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